Author

D. Remus

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 2 Biophysics· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:chromatin & epigenetic regulation· 3 Organism:yeast· 3 Research Focus:cell signaling & trafficking· 1 Assay:ChIP-seq· 1 Research Focus:development & morphogenesis· 1 Assay:DNA methylation· 1 Research Focus:protein structure prediction· 1

Frequent Co-Authors

A. E. Ikui· 1 shared A. Silva· 1 shared C. Kumar· 1 shared J. C. Castaneda· 1 shared J. F. X. Diffley· 1 shared J. Griffith· 1 shared J. Philip· 1 shared M. Loog· 1 shared

Activity by Year

2020-2021 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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1 shared paperCell Biology

A. E. Ikui

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Cdc6 is sequentially regulated by PP2A-Cdc55, Cdc14 and Sic1 for origin licensing in S. cerevisiae

J. Philip, M. Ord, A. Silva, S. Singh, J. F. X. Diffley, D. Remus, M. Loog, A. E. Ikui

This study identifies the sequential regulation of Cdc6 phosphorylation by PP2A-Cdc55, Cdc14, and Sic1 in S. cerevisiae to control origin licensing.

bioRxiv · Sep 14, 2021Cell Biology

Mechanisms of loading and release of the 9-1-1 checkpoint clamp

J. C. Castaneda, M. Schrecker, D. Remus, R. K. Hite

The paper presents structures of the yeast checkpoint clamp loader, Rad24-RFC, in complex with 9-1-1 and a 5' junction, revealing mechanisms of 9-1-1 recruitment and release.

bioRxiv · Sep 13, 2021Biophysics

The interplay of RNA:DNA hybrid structure and G-quadruplexes determines the outcome of R-loop-replisome collisions

C. Kumar, S. Batra, J. Griffith, D. Remus

This study investigates how RNA:DNA hybrid structures and G-quadruplexes influence R-loop-replisome collisions, showing structural differences determine replication outcomes.

bioRxiv · Jul 16, 2021Biochemistry

Antagonistic control of DDK binding to licensed replication origins by Mcm2 and Rad53

S. Abd Wahab, D. Remus

The paper identifies Mcm2's N-terminal tail as promoting DDK recruitment to replication origins and shows Rad53 inhibits DDK binding through steric effects, revealing a checkpoint-dependent origin inhibition mechanism.

bioRxiv · May 4, 2020Biochemistry